. Introduction
Plastic
was created to enhance human living conditions, but it now poses a serious
threat to the planet's safety and environment (1,2). Artificial
materials made of high molecular weight molecules, known as polymers, either
naturally occurring or synthesized, are referred to as "plastics". Plastics have been widely employed
in a variety of industries because of their affordability, adaptability, strength,
durability, and lightweight(3,4). Additives
are added to plastic during production to give it particular qualities (5).
Polypropylene (PP), polyethylene (PE), polyethylene terephthalate (PET),
polystyrene (PS), polyvinyl chloride (PVC) and others are major commercial
plastics on the market (2,6,7).Numerous
sources contribute to plastic trash's direct and indirect accumulation in
aquatic ecosystems (8). According
to (7), a high
yield and low recovery indicate that a significant amount of plastics end up in
the environment. Plastic remains in the aquatic environment because it is
designed to be long-lasting. Plastic polymers can, however, be broken down
gradually by heat, oxidation, light, hydrolysis or microbes (such as Bacillus
cereus, Micrococcus sp., or Corynebacterium) (9). Plastic
splits and fragments due to thermal stress caused by temperature changes.
Examples of plastic degradation and MP generation include the disintegration of
plastic bags and packaging containers, the dispersal of synthetic fibers from
garments and the breaking up of plastic bottles and containers (10).Synthetic substances with a high
molecular weight that have been micronized into plastic particles smaller than
5 mm are known as microplastics (11). Primary and secondary
microplastics are distinguished by whether the particles were created with that
size in mind (primary) or are the consequence of larger objects breaking down
(secondary). Plastic nanoparticles utilized in various industrial processes,
plastic powders used in molding, micro-beads used in cosmetic formulation and
industrial "scrubbers" used to blast clean surfaces are examples of
primary microplastics. Secondary microplastics are formed when bigger plastic
products are fragmented and weathered. This can occur while materials like
paint, tires and textiles are being used or after they have been released into
the environment (12,13).
Figure 1: Sources, fate and effects of microplastic in aquatic environment.
Organisms interact with
microplastics at different trophic levels and interaction can happen through a
variety of pathways. While microplastics present in the environment (water or
sediment) directly expose organisms, those ingested by prey may indirectly
contaminate predators through trophic transfer (14,15). Fish is considered as a good
source of protein all over the world. A
recent WorldFish and Indian
Council of Agricultural Research study on fish consumption patterns
shows that from 2005 to 2021 there was an 81.43% increase in per capita fish
consumption in India, along with a 32% growth in the fish-consuming population (16). Water bodies are being polluted by microplastics
which ultimately affects the life of aquatic organisms including fishes.
Microplastics have a variety of effects on fish health, either by themselves or
when combined with other environmental pollutants. Fish exposed to these
pollutants experience reductions in growth, oxidative stress, immunotoxicity,
neurotoxicity, inflammation, organ damage, physical harm, and behavioral changes
(17). According to (13), the discovery of microplastics in
every aquatic compartment has led to their recognition as a ubiquitous
contaminant, posing a threat to both aquatic life that consumes them and humans
who consume fisheries products. This review aims to examine the effects of
microplastic exposure on fish physiology, focusing on accumulation, organ
function, and potential implications for reproductive health.
2. Materials and Methods
We conducted a systematic
literature review. Search engines such as Google Scholar, NCBI PubMed,
ResearchGate, ScienceDirect, and SpringerLink have been used to search
literature relevant to the topic. The keywords, such as “microplastic effects
on fish," "fishes," "physiology,"
"reproduction," and “cytotoxicity in fish,” were used in various
combinations during the literature search. Most of the publications searched
were in environmental science, agriculture and biological sciences, and earth
and planetary sciences. After screening 200 papers, 74 were chosen for
reference by eliminating those that were unrelated to our study.
2.1 PHYSIOLOGICAL EFFECTS OF
MICROPLASTIC ON FISH
With the prevalence of small-sized
particles, such as microplastics in everyday products (ingredients in many
daily use items, cosmetics, packaging, and so on) and nanoparticles in drugs,
the biomedical field, and various formulations, there are growing concerns
about their negative impact on aquatic life. Their small size makes them easily
consumed by a wide range of species, from zooplankton to larger marine mammals.
Because these pollutants have the potential to directly or indirectly penetrate
the environment and contaminate soil, water, and air, it is now important to
comprehend how they interact and impact the aquatic biota in their natural
habitat (18). Fish are the primary vertebrate
organisms utilized for monitoring microplastics (MPs), likely due to their
higher exposure levels to these particles. MPs can enter fish through various
routes, including their gills and the consumption of food and water (19, 20).
Figure 2: Physiological alterations in fish after microplastic exposure.
Toxicity
and cellular damage:
MPs
are tiny pieces of plastic that are commonly found in aquatic ecosystems all
around the world. There have been reports of physiological problems in fish
exposed to MPs, including oxidative stress, neurotoxicity, and immunotoxicity (21). Particle
toxicity, inflammation, and oxidative stress all contribute to cytotoxicity (13,22). Severe
organ malfunction and disease may arise from cell toxicity brought on by
environmental pollutants and medications. According to recent research, the
primary mechanisms of cell toxicity include DNA damage, mitochondrial
malfunction, oxidative stress brought on by ROS, and excessive NO generation (23).MPs were
found to be cytotoxic due to oxidative damage and inflammation (24).
Microplastics can induce oxidative stress by releasing reactive oxygen species
(ROS) produced during the inflammatory response and oxidizing substances (like
metals) that were previously adsorbed on their surfaces (13,25).The
interaction between MPs and cellular components can affect cell signaling,
which in turn can activate the processes of autophagy, apoptosis, and
proteolysis. Oxidative stress causes metabolic changes in fish tissues. MPs'
distribution and accumulation in fish liver and gills have a significant impact
on tissue toxicity (26). "Aged"
microplastics can activate the antioxidant defense mechanisms and have an
impact on the cellular health of freshwater fish species Percafluviatilis(27).
Long-term exposure to microplastics can cause immune cell dysfunction, necrosis,
chronic flogosis, and cell proliferation in organisms (9,13).In
zebrafish, PE-MPs can significantly alter the activity of Na+/K+-ATPase and
antioxidant enzymes (28). Both
microplastics and mercury independently induced neurotoxicity via
acetylcholinesterase (AChE) inhibition, lipid peroxidation in neural and
muscular tissues, and alterations in the activity of energy-related enzymes
lactate dehydrogenase (LDH) and isocitrate dehydrogenase (IDH) (29,30). The
association between zinc oxide nanoparticles (ZnO-NPs)andpolyethylene
microplastic (PE-MPs) exacerbates and raises serious
health difficulties in aquatic forms. Therefore, for the sake of environmental
safety, the release of these particles must be controlled. More research is
needed to better understand the toxicity mechanism of the interaction in fish (18).
Effects on the immune system:
Microplastics
or nanoplastics may change organismal defense mechanisms, which could disrupt
innate immune responses in fish populations. Fish larvae may experience harm to their sense of
smell as a result of an immunological reaction brought on by microplastic
pollution. Furthermore, it has been demonstrated that POPs are
absorbed by plastic fragments present in marine environments. Therefore,
absorbed ambient chemicals, plastic-associated compounds, and particle toxicity
can impact the immune system (31). The
immunological, digestive, and reproductive systems are all affected by virgin
MPs and nanoparticles (NPs), which also cause intestinal dysbiosis and may have
generational implications (32). Fishes may experience stress from
microplastics, which could interfere with their natural defenses. They
can also cause immune cells to have less phagocytic activity, less cell
viability, and lysosomal membrane degradation (33,34).Exposure to
microplastics can also influence the activation of pro-inflammatory cytokines
and induce inflammation (34,35). MP
accumulation and goblet cell growth was discovered in the stomach of a young
guppy following a 28-day exposure to MPs(36). MPs
lowered the function of digestive enzymes and raised immune cytokine levels in
the gut.High quantities of MPs cause cellular immunological stress in yellow
catfish, and hypoxia intensifies these effects on immune parameters (37). According
to(38),
microplastics can trigger an inflammatory response by upregulating
pro-inflammatory cytokines. They demonstrate that MPs may affect the
immunological response and antioxidant system of GIFT (Genetically Improved
Farmed Tilapia), a strain of Nile tilapia (Oreochromisniloticus). Fish exposed to microplastics
showed elevated brain AChE activity and lipid oxidative damage to their brain,
muscles and gills (39).
Effects on the respiratory and
circulatory system:
The
degree of direct ionoregulatory disruption caused by microplastics varies
according to the type, size, concentration, and exposure schedule of the microplastics
(40).Compared to
the specimens that tested negative for MP ingestion, the gills of the
MP-ingested animals displayed greater LPO levels and a higher index of lipid peroxidation
damage (39,41).Damage
caused by gill lipid peroxidation might have negative consequences, such as
impaired respiration and xenobiotic biotransformation (41,42).Although
microplastics have no direct effect on C.
gariepinus survival, their buildup in fish tissues increases the fish's
opercular respiratory rate (ORR) and decreases its swimming speed, which may
have an impact on the fish's capacity for foraging and make them more
vulnerable to predators(43). In (44),
histological analyses were conducted after exposing early juvenile tilapia
(Oreochromis niloticus) to MPs. Complete lamellar fusions, lifting of the
epithelium, shortening, and degeneration of secondary lamellae, hyperplasia,
blood vessel dilatation, and congestion, and MP deposition between primary
lamellae were all observed in the gill tissue.
Polyethylene
(PE) microplastics accumulate in certain organs,
affecting the hematological parameters, plasma components, and antioxidant
response of juvenile P. fulvidraco.
Every physiological change brought on by acute exposure to PE-MPs was
concentration-dependent (45). After
zebrafish were exposed to sublethal quantities of Polystyrene
microplastics (PS-MPs), there was a decrease in heart
rate, an increase in oxidative stress through the stimulation of associated
parameters that led to autophagy and apoptosis, metabolic changes in the heart,
and a decrease in fish activity. Cardiotoxicity has been noted in fish, and
several forms of plastic have been shown to accumulate in the heart, indicating
a trophic transfer through the bloodstream. The circulatory system of a fish
may be impacted by plastic pieces at various stages of its life cycle. Indeed,
morphological modifications and variations in heart rate were noted in embryos
and larvae following maternal transfer (46).
Effects
of Microplastic on various fish species:
|
Types of
microplastic
|
Name of organism
|
Findings
|
Ref.
|
|
Polystyrene
microplastics (PS-MPs)
|
Goldfish (Carassius
auratus)
|
The results of this study
demonstrated the size-dependent toxicity of polystyrene microplastic on the
antioxidant defense system and the histology of the goldfish's intestine,
liver, and gills.
|
(47)
|
|
Polystyrene
microplastics (PS-MPs)
|
Japanese
medaka (freshwater fish) and Java medaka (marine fish),
|
There were few negative impacts on
medaka's survival, development, and reproduction after exposure to PS-MPs at
107 beads/L. According to next-generation sequencing data, the buildup of MPs
may still have an impact on fish cell adhesion, toxin metabolism, and other
processes.
|
(48)
|
|
Polyethylene Microplastics (PE-MPs) and
ZnOnanoplastic
|
Mosquito Fish
(Gambusiaholbrooki)
|
PE-MPs promote oxidative stress
and ZnO-NP-induced toxicity in fish. There was a notable decrease in total
antioxidant (TAN) levels.
ZnO-NPs by themselves and in
conjunction with PE-MPs were found to significantly increase the activity of
catalase, superoxide dismutase, glutathione peroxidase, and glutathione
reductase levels.
|
(18)
|
|
Fluorescence
red polymer microspheres and Mercury
|
European
seabass,
(Dicentrarchuslabrax)
|
Microplastics may
have absorbed mercury from water, leading to its bioaccumulation in
fish tissues. In addition to causing neurotoxicity and lipid peroxidation in
the brain and muscles, microplastics and mercury also altered the
activity of the energy-related enzymes isocitrate dehydrogenase (IDH) and lactate
dehydrogenase (LDH).
|
(29)
|
|
Polyethylene,
polyester
and semisynthetic cellulose (rayon)
|
European seabass
(D. labrax), the Atlantic horse mackerel (T. trachurus)
and
Atlantic chub mackerel (S. colias)
|
Fish exposed to microplastics
showed lipid oxidative damage in the brain, muscle, and gills, as well as
elevated brain AChE activity.
|
(39)
|
|
Polyethylene
microplastic
|
African
Catfish (ClariasGariepinus)
|
Consumption of MPs caused
testicular injury, decreased sperm quality and viability, and reduced hormone
levels.
Lycopene and Chlorella supplements effectively detoxified MP-induced
reproductive impairment in male catfish, while citric acid was ineffective.
|
(49)
|
|
Polyethylene
|
Atlantic cod (Gadusmorhua)
|
The addition of 1% polyethylene
MPs at 0.3–0.6 mm had no effect on the Atlantic cod's fecundity or egg
quality metrics during spawning, nor on feed intake, nutrient digestibility,
or biometric assessments throughout maturation.
|
(50)
|
|
Polystyrene microplastics
|
Medaka fish (Oryziaslatipes)
|
MP-related variations in the
number of gravid females, fecundity, and fertilization rates were observed in
the early days of the reproductive phase. In the days that followed, these
values generally returned to their typical rates.
Other organs showed mild
alterations, including anomalies in thyroid follicular thickness and size,
glomerular and tubular modifications in the kidneys, and increased fluid in
the peritoneal cavity.
|
(51)
|
|
Polystyrene
microplastics
|
Zebrafish (Daniorerio)
|
Zebrafish female reproduction is
hampered by PS-MP exposure because it causes oxidative stress, apoptosis, and
hormonal instability through SIRT1 regulation.
|
(52)
|
|
Microbeads
|
Tilapia
(Oreochromisniloticus)
|
Histopathology revealed congestion
of blood capillary in the kidney, deformation of hepatocytes, degenerated acini with pyknotic nuclei, complete
lamellar fusions and deformed notochord. MPs can cause metabolic changes in
individual cells or tissue lesions, impacting fish health and survival.
|
(44)
|
|
Polystyrene
microplastics
|
Grass
carp (Ctenopharyngodonidella)
|
While MP particles with small size
and high concentration generated more severe hepatic congestion and higher
oxidative stress, MP particles with big size and high concentration caused
more severe intestine damage and less weight gain.
|
(53)
|
|
Polystyrene
microplastics
|
Guppy
(Poeciliareticulata)
|
MPs increased the amounts of
immune cytokines in the gut and decreased the activity of digesting
enzymes. Exposure to MPs led to an increase in Proteobacteria at the
phylum level and a decrease in the diversity and evenness of the gut
microbiota.
|
(36)
|
|
Raw
powder
|
Tilapia (Oreochromis
niloticus)
|
MPs caused male tilapia to develop
testis-ova, experience oxidative stress, hormonal disturbance, and testicular
injury.
|
(54)
|
|
Polypropylene microplastics
|
Mozambique
tilapia
(Oreochromismossambicus)
|
In liver tissues, exposure to
microplastic increased DNA damage and cell death.
Hepatocyte necrosis and vacuole formation, atrophy of dilated sinusoids in
the liver, and a decrease in leukocyte infiltration of sinusoids were among
the morphological alterations.
|
(55)
|
|
Polystyrene
microplastics
|
Zebrafish (Daniorerio) and perch (Percafluviatilis
|
PS-MPs causes oxidative
stress on the liver and gills of the two fish species under study, as
evidenced by assessments of DNA damage, protein oxidation, and lipid
peroxidation.
Cell signaling is also affected, which leads to molecular inductions such as
apoptosis, ubiquitylation, autophagy, and metabolic changes that primarily
impact the metabolism of amino acids, nitrogen, and energy.
|
(26)
|
|
High-density polyethylene (HDPE) microplastics
|
Zebrafish (Daniorerio)
|
Large MPs (size 120 μm) physically
impact the lateral line system of zebrafish by directly harming hair cells,
while tiny and medium MPs' digestible size results in stomach damage and
metabolic repercussions.
|
(56)
|
|
Polyethylene
microplastic
|
Korean Bullhead, (Pseudobagrusfulvidraco)
|
High PE-MP exposure changed
several plasma components and caused a marked decline in hematological parameters,
including RBC count, Hb concentration, and hematocrit (Ht) value.
|
(45)
|
|
Polyamides
(PA), polyethylene (PE), polypropylene (PP),
polyvinyl chloride (PVC) and polystyrene (PS) particles
|
Zebrafish
(Daniorerio)
|
Intestinal injury from
microplastic particles included enterocyte splitting and villi cracking.
|
(57)
|
|
Polystyrene,
green fluorescent microsphere
|
Yellow Catfish
(Pelteobagrusfulvidraco)
|
The detrimental effects of MPs on
the expression of immunological markers in yellow catfish were exacerbated by
the interaction between hypoxia and MPs.
|
(37)
|
|
Polystyrene
microplastic Green Fluorescent microspheres
|
Grass carp (Ctenopharyngodonidella)
|
MPs resulted in hepatocellular
vacuolization and metabolic problems.
High concentrations of MPs resulted in increased CYP1A1 levels, oxidative
stress, and inhibition of the SOD-CAT antioxidant system.
|
(58)
|
|
Polystyrene
microplastics
|
Zebrafish (Daniorerio)
|
PS-MPs may cause oxidative stress
and histological alterations in fish liver.
|
(59)
|
|
Polyethylene
microplastic
|
Zebrafish (Daniorerio)
|
Changes in cyp 1a and vtg 1
expression levels indicate impacts on the AHR pathway and disrupted
oogenesis. Acute exposure causes neurotoxicity.
|
(60)
|
|
Polyethylene
microplastic
|
European perch (Percafluviatilis)
|
In comparison to virgin PE-MPs,
uptake of "aged" PE-MPs resulted in a stronger reaction and, hence,
greater toxicity.
|
(27)
|
|
Polystyrene
microplastics
|
Zebrafish (Daniorerio)
|
Polystyrene microplastic
accumulated in zebrafish intestines, resulting in significant variations in
steroidogenic mRNA expression.
Reproductive success and parental health were mainly unaffected.
Transgenerational impacts were deemed insignificant.
|
(61)
|
|
Polyethylene
microplastic
|
Zebrafish (Daniorerio)
|
An increase in Na+/K+-ATPase
activity is a possible method to manage the ionic loss driven by the
oxidative stress caused by MPs.
|
(28)
|
|
Low-density
polyethylene (LDPE) microplastic
|
Seabream (Sparusaurata)
|
The general social and feeding
behavior of seabream appeared to be impacted by MP.
MPs causes a physiological reaction
in the tissues of the brain and liver.
|
(62)
|
|
Polyethylene
microplastics
|
Zebrafish (Daniorerio)
|
Exposure to pristine or
contaminated polyethylene microplastics can harm fish growth and reproductive
performance and generate an impact that lasts
|
(63)
|
|
Polyethylene
microplastics
|
African catfish (Clariasgariepinus)
|
The accumulation of microplastics
in fish tissues increased opercular respiratory rate (ORR) and decreased
swimming speed, potentially affecting the fish's foraging capacity and
increasing their susceptibility to predation.
|
(43)
|
|
Polystyrene
microplastics
|
Marine medaka (Oryziasmelastigma)
|
The colon, liver, gonad, and gills
all experienced histological alterations and oxidative stress.
Microplastics altered the HPG axis
and steroidogenesis pathway in a sex-dependent manner, affecting hormone balance,
gonad maturation, and offspring development.
|
(64)
|
|
Polystyrene
microplastics
|
Marine medaka (Oryziasmelastigma)
|
Exposure to MPs cause rapid sexual
maturity, decreased hatching success, and suppression of body size and
gonadosomatic index (GSI ).
|
(65)
|
|
Polyethylene microplastics
|
Loach
(Paramisgurnusdabryanus)
|
PE-MPs impact the immunological
and antioxidant systems (TLR–NF–κB pathway), disrupt the HPG axis-mediated
sex hormone balance, and cause histological changes in the gonads, all of
which have an impact on gametogenesis and reproduction.
|
(66)
|
|
Fluorescent
polystyrene microplastics
|
Bighead
carp (Aristichthysnobilis), hybrid snakehead (Channamaculata×Channaargus)
and Indian major carp, mrigal (Cirrhinusmrigala)
|
Compared to filter feeders and
omnivores, carnivores consumed fewer microplastics.Filter feeders were better
at removing microplastics than omnivores.
|
(67)
|
|
Polypropylene microplastic
|
Largemouth
bass (Micropterussalmoides)
|
Exposure to MPs affected
intestinal morphology and the recombination process but had no discernible effect
on the variety or composition of the intestinal microbial population.
|
(68)
|
|
Polypropylene microplastic
|
Zebrafish (Daniorerio)
|
Microplastic fibers may affect
zebrafish by increasing glycerophospholipid metabolism, causing oxidative
damage and inflammation, and decreasing fatty acyl metabolism due to
nutritional deficit.
|
(69)
|
|
Polystyrene
microplastics
|
Nile tilapia (Oreochromisniloticus)
|
MPs have been shown to increase
ROS generation and disrupt the antioxidative enzyme system in genetically
improved farmed tilapia (GIFT), particularly in the
brain.
|
(38)
|
Effects on the digestive system:
Satiety
is one of the initial impacts of MP consumption, which alters the body's eating
habits. As a result, a decrease in food intake is typically seen (2,70–73).
Exposure to microplastic produced
varying degrees of detrimental effects on fish liver function, including
oxidative stress from free radicals, liver lipid metabolism problems, immune
system impairment, and liver tissue damage and inflammation (74).According to (57) microplastic particles of PA, PE,
PP, PS, and PVC damaged D. rerio's
digestive tract by causing enterocyte splitting and villi cracking.MPs can harm
fish physically by causing internal abrasions and digestive tract blockages.
Poor health, poorer digestion, and decreased vitamin absorption can result from
this. It was discovered that MPs could interfere with fish metabolism and
hormonal balance (18).MPs can accumulate in fish's digestive
tracts as a result of absorption, leading to gastrointestinal tract perforation
or a false sense of satiety that makes them hungry. These MPs have detrimental
effects on fish's bodies and physiologies (75).Although microplastic exposure may
partially impact intestinal shape and the intestinal microbial community's
recombination process, it had no discernible effect on the diversity or
composition of the intestinal microbial community(68).However, microplastics can upset
intestinal flora, changing the ratio of beneficial bacteria to dangerous ones (34,76).
Different MP concentrations caused
metabolic problems and hepatocellular vacuolization in grass carp (58). In the digestive tract of
zebrafish, microplastics cause fat accumulation and liver inflammation (59). MPs usually interfere with the
liver's ability to metabolize energy, lipids, and glucose (69). Physiological issues of goldfish
(Carassiusauratus) are influenced by the size of microplastics, particularly
polystyrene(47). Histological damage was found in
the fish's liver, intestine, and gills after exposure to the microplastic. Both
the dosage and the size of the microplastic were found to have an impact on the
severity of these lesions. Omnivorous and carnivorous fish are more likely to
ingest microplastics in freshwater and marine environments, according to
contamination based on eating practices(77). In freshwater fish, polyethylene
terephthalate was the most common plastic polymer, whereas in marine fish,
Polyethylene was the most common.While MP particles with a small size and
high concentration caused more severe oxidative stress and hepatic congestion,
MP particles with a big size and high concentration caused more severe intestinal
damage and less weight gain (53).
Effects on reproductive health:
Fish are severely harmed by MPs,
which affect their development, survival, and ability to reproduce. Compared to
freshwater fish, marine fish exhibit a higher tolerance to MPs in terms of
growth and reproduction(78). In (48), the effects of polystyrene
microplastics (PS-MPs) on survival, reproduction, body weight, and gene
expression in Japanese medaka was investigated.During the first few days of the
reproductive season, medaka fish (Oryziaslatipes)
showed MP-related differences in fecundity, fertilization rates, and the number
of gravid females. Over the next few days, these numbers returned to their
typical rates. There were no discernible impacts of polystyrene MP exposure on
the success of the progeny (51). Microplastics result in delayed
gonadal maturation, diminished body mass, and hastened female sexual maturity
in marine medakas. The histological study indicated modifications in the
structure of gill lamellae and abnormalities in the gonads (51,64,65). Exposure to PS-MPs negatively
impacted fertilization and significantly changed the gonadosomatic index (GSI)
in zebrafish(52). The female
hypothalamus-pituitary-gonadal (HPG) axis was negatively regulated by
microplastics. Incubation was delayed, and the offspring's body length, heart
rate, and hatching rate all decreased when their parents were exposed to 20
μg/L of microplastics(64).
The harmful effects of microplastic
on Nile tilapia (Oreochromesniloticus)
was investigated and it was found that the fish subjected to MP developed
testicular, histological, degenerative, and testis-ova alterations(54). In adult zebrafish, acute exposure
to microplastics such as PE can disrupt oogenesis, change the aryl hydrocarbon
receptor (AHR) pathway, and result in neurological or behavioral problems(60).Males treated with microplastic had
significantly higher mortality, shorter standard length, smaller body area,
fewer sperm bundles and sigmoid displays, and lower levels of sexual interest(79). 1% of MPs recovered from the sea
after natural weathering affected gonadal development, digestion, and
reproductive endocrinology (i.e., successful fertilization and egg production)
in Atlantic cod from early maturation to spawning(50).Microplastics made of polythene
significantly harm population sustainability and affect reproduction, claim (66). The effects of parental exposure
to polystyrene microplastic on zebrafish spawning, fertilization, survival, and
offspring growth were investigated by(61). Polystyrene microplastics (PS-MPs)
damage the female reproductive system and the processes that cause reproductive
toxicity(80).
According to (63), fish exposed to pristine or
contaminated polyethylene microplastics in their diet for an extended period
may experience problems with growth and reproduction and affect future
generations.MP contamination in the aquatic environment can have a direct
effect on the reproductive function of freshwater fish, including the African
catfish. MP consumption may contribute to reproductive stress, and reproductive
toxicity in male catfish. For example, testicular injury, reduced sperm quality
and viability and suppressed hormonal profiles were observed (49). Species-specific reproductive
responses to microplastic exposure varied, but all showed a significant
decrease in fertility, sperm swimming speed, gamete and oocyte quality and
offspring quality (33).
3. CONCLUSION
In
conclusion, we pinpoint areas of unmet knowledge that require more study, such
as examining the potential consequences of microplastic exposure on future
generations and measuring the positive and negative interactions between MPs
and other ecological contaminants. This increased understanding of the possible
consequences of MPs on aquatic wildlife is expected to help policymakers design
mitigation policies to preserve aquatic species. More long-term studies are
needed to assess chronic effects on fish populations and ecosystems.